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        <title>Kalain Hündin bioinfo</title>
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       <dc:date>2026-05-06T02:56:19+00:00</dc:date>
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        <description>Here we will use the BWA aligner to map short reads to a reference genome, and then call variants (differences between the reads and the reference).

Download data

Goal: get the sequence data!

Run:
   mkdir ~/data
   cd ~/data
   curl -O http://dib-training.ucdavis.edu.s3.amazonaws.com/2017-ucdavis-igg201b/SRR2584857.fq.gz</description>
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        <dc:date>2023-09-12T23:15:34+00:00</dc:date>
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        <title>bioinfo:oneliners</title>
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        <description>for filename in *.fa; do sed -i '/&gt;Recurrent fasta name/c\&gt;'$filename'' $filename; done


all VCF to vcf.gz



ls *.vcf | xargs -n1 -P0 bgzip


AWK


awk '{if(NR%4==2) {count++; bases += length} } END{print bases/count}' &lt;fastq_file&gt;

# keep online lines with col 5 &amp; 4 of length == 1char

zgrep -v &quot;\.\/\.:\.&quot; Merged.vcf.gz | awk '{if (length($5)==1 &amp;&amp; length($4)==1) print $line}'</description>
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